Canonical Allele Identifier: CA2631426720
Gene: CREBBP HGNC NCBI

Linked Data

gnomAD v4: 16-3777567-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3777567G>C , CM000678.2:g.3777567G>C GRCh38
NC_000016.9:g.3827568G>C , CM000678.1:g.3827568G>C GRCh37
NC_000016.8:g.3767569G>C NCBI36
NG_009873.1:g.107554C>G
NG_009873.2:g.108147C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.2158+46C>G MANE Select ENSP00000262367.5:n.2158+46C>G
ENST00000262367.9:c.2158+46C>G ENSP00000262367.5:n.2158+46C>G
ENST00000382070.7:c.2044+46C>G ENSP00000371502.3:n.2044+46C>G
ENST00000570939.2:c.763+46C>G ENSP00000461002.2:n.763+46C>G
ENST00000571826.5:c.207+46C>G
ENST00000572134.1:c.426+444C>G
NM_001079846.1:c.2044+46C>G NP_001073315.1:n.2044+46C>G
NM_004380.2:c.2158+46C>G NP_004371.2:n.2158+46C>G
XM_005255124.3:c.2113+444C>G XP_005255181.1:n.2113+444C>G
XM_005255125.3:c.2158+46C>G XP_005255182.1:n.2158+46C>G
XM_006720848.2:c.2158+46C>G XP_006720911.1:n.2158+46C>G
XM_011522380.1:c.2104+46C>G XP_011520682.1:n.2104+46C>G
XM_011522381.1:c.1405+46C>G XP_011520683.1:n.1405+46C>G
XM_011522382.1:c.2158+46C>G XP_011520684.1:n.2158+46C>G
XM_005255124.4:c.2113+444C>G XP_005255181.1:n.2113+444C>G
XM_005255125.4:c.2158+46C>G XP_005255182.1:n.2158+46C>G
XM_006720848.3:c.2158+46C>G XP_006720911.1:n.2158+46C>G
XM_011522381.2:c.1405+46C>G XP_011520683.1:n.1405+46C>G
XM_011522382.3:c.2158+46C>G XP_011520684.1:n.2158+46C>G
XM_017022944.1:c.2158+46C>G XP_016878433.1:n.2158+46C>G
NM_004380.3:c.2158+46C>G MANE Select NP_004371.2:n.2158+46C>G